Evidence map›Paper›PMID 15334067›Full record

ArticleOncogene2004

Mechanistic aspects of mda-7/IL-24 cancer cell selectivity analysed via a bacterial fusion protein.

Moira Sauane, Rahul V Gopalkrishnan, Heng-Tong Choo, Pankaj Gupta, Irina V Lebedeva, Adly Yacoub, Paul Dent, Paul B Fisher

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 66 citations in OpenAlex.

  1. Interleukin-24 Immunobiology and Its Roles in Inflammatory Diseases.International journal of molecular sciences · 2022
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. MDA-7/IL-24: multifunctional cancer killing cytokine.Advances in experimental medicine and biology · 2014
    Review
  10. Article
  11. Article
  12. IL-24 sensitizes tumor cells to TLR3-mediated apoptosis.Cell death and differentiation · 2013
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Moira SauaneDepartment of Pathology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, College of Physicians and Surgeons, New York, NY 10032, USA.
Rahul V Gopalkrishnan
Heng-Tong Choo
Pankaj Gupta
Irina V Lebedeva
Adly Yacoub
Paul Dent
Paul B Fisher
Columbia University Irving Medical Center · USVirginia Commonwealth University · USColumbia University · US

Funding

SIGNALING PATHWAYS REGULATING EPITHELIAL CELL SURVIVALR01DK052825 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 1999 to 2013
$3.3M
MDA-7: Novel Cancer Therapeutic GeneR01CA097318 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2002 to 2012
$2.8M
Role of TRRAP in the p53-Mediated Transcription of mdm2R01CA098172 · NCI · WISTAR INSTITUTE · PI MCMAHON, STEVEN B · 2003 to 2007
$1.4M
Carcinoma cell radiosensitization by MAPK inhibitionR01CA088906 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENT, PAUL · 2001 to 2004
$783k
NCI NIH HHS CA097318NCI NIH HHS CA098172NCI NIH HHS CA88906NIDDK NIH HHS DK52825
6 · The paper itself

Abstract

The human mda-7/IL-24 gene product is normally expressed in melanocytes and certain lymphocyte populations. Loss of expression, a distinctive feature of many tumor suppressor genes, has been documented at RNA and protein levels in association with melanoma progression both in vitro as well as in human tumor-derived material. The MDA-7/IL-24 protein undergoes post-translational processing, including removal of an amino-terminal 48-residue signal peptide and extensive glycosylation prior to its secretion by producing cells. Its inherent cytokine properties have been documented in multiple reports, which have identified and characterized its cognate receptors and activation of the JAK/STAT signaling pathway following ligand/receptor docking. A notable and incompletely understood property of MDA-7/IL-24 is its ability to induce apoptosis in transformed cells, while having marginal growth suppressive effects on normal primary or immortalized cell lines. MDA-7/IL-24 has been delivered to cells, tumor xenografts and patients in clinical trials via a nonreplicating adenovirus (Ad.mda-7). Studies utilizing eukaryotically expressed and purified MDA-7/IL-24 protein from several sources have recapitulated some of the molecule's reported properties including receptor binding and JAK/STAT activation. Here, we report the properties and characteristics of a bacterially expressed and purified GST-MDA-7 fusion protein. These studies reveal that GST-MDA-7 retains its cancer-selective apoptosis-inducing properties, thereby providing a new reagent that will assist in defining the mechanism of action of this novel cytokine. In addition, retention of tumor-specific activity of GST-MDA-7 suggests that this protein may also have therapeutic applications.

Indexed as

AnimalsApoptosisBreast NeoplasmsCell Line, TumorFemaleGenes, Tumor SuppressorGenetic TherapyGlutathione TransferaseHumansInterleukin-24InterleukinsRecombinant Fusion ProteinsSignal TransductionTransplantation, HeterologousGlutathione TransferaseInterleukin-24InterleukinsRecombinant Fusion Proteins

Identifiers

PMID15334067
OpenAlexW2081823691

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.